These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

155 related articles for article (PubMed ID: 18980857)

  • 1. Mutational screening of the mitochondrial transcription factors B1 and B2 (TFB1M and TFB2M) in Parkinson's disease.
    Sánchez-Ferrero E; Coto E; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; Alvarez V
    Parkinsonism Relat Disord; 2009 Jul; 15(6):468-70. PubMed ID: 18980857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.
    Alvarez V; Corao AI; Sánchez-Ferrero E; De Mena L; Alonso-Montes C; Huerta C; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; García-Castro M; Coto E
    Neurosci Lett; 2008 Feb; 432(1):79-82. PubMed ID: 18248889
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.
    Belin AC; Björk BF; Westerlund M; Galter D; Sydow O; Lind C; Pernold K; Rosvall L; Håkansson A; Winblad B; Nissbrandt H; Graff C; Olson L
    Neurosci Lett; 2007 Jun; 420(3):257-62. PubMed ID: 17537576
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Mitochondrial transcription factor A variants and the risk of Parkinson's disease.
    Gaweda-Walerych K; Safranow K; Maruszak A; Bialecka M; Klodowska-Duda G; Czyzewski K; Slawek J; Rudzinska M; Styczynska M; Opala G; Drozdzik M; Kurzawski M; Szczudlik A; Canter JA; Barcikowska M; Zekanowski C
    Neurosci Lett; 2010 Jan; 469(1):24-9. PubMed ID: 19925850
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
    Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
    Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mitochondrial DNA depletion and its correlation with TFAM, TFB1M, TFB2M and POLG in human diffusely infiltrating astrocytomas.
    Correia RL; Oba-Shinjo SM; Uno M; Huang N; Marie SK
    Mitochondrion; 2011 Jan; 11(1):48-53. PubMed ID: 20643228
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease.
    Günther C; von Hadeln K; Müller-Thomsen T; Alberici A; Binetti G; Hock C; Nitsch RM; Stoppe G; Reiss J; Gal A; Finckh U
    Neurosci Lett; 2004 Oct; 369(3):219-23. PubMed ID: 15464268
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.
    Huerta C; Castro MG; Coto E; Blázquez M; Ribacoba R; Guisasola LM; Salvador C; Martínez C; Lahoz CH; Alvarez V
    J Neurol Sci; 2005 Sep; 236(1-2):49-54. PubMed ID: 15975594
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Characterization of the mouse genes for mitochondrial transcription factors B1 and B2.
    Rantanen A; Gaspari M; Falkenberg M; Gustafsson CM; Larsson NG
    Mamm Genome; 2003 Jan; 14(1):1-6. PubMed ID: 12532263
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Prokaryotic expression and purification of mitochondrial transcription complex proteins].
    Liu G; Yang RF; Shi BY; Liu DP
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2011 Dec; 33(6):638-43. PubMed ID: 22509547
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The transcription factor PITX3 is associated with sporadic Parkinson's disease.
    Fuchs J; Mueller JC; Lichtner P; Schulte C; Munz M; Berg D; Wüllner U; Illig T; Sharma M; Gasser T
    Neurobiol Aging; 2009 May; 30(5):731-8. PubMed ID: 17905480
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Examination of the MSX1 gene in patients with Parkinson's disease.
    Deng H; Zhu SH; Le WD; Yang HR; Lv HW; Xu HB; Xie WJ; Jankovic J
    Acta Neurol Scand; 2009 Dec; 120(6):442-4. PubMed ID: 19922584
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.
    Palacín M; Alvarez V; Martín M; Díaz M; Corao AI; Alonso B; Díaz-Molina B; Lozano I; Avanzas P; Morís C; Reguero JR; Rodríguez I; López-Larrea C; Cannata-Andía J; Batalla A; Ruiz-Ortega M; Martínez-Camblor P; Coto E
    Mitochondrion; 2011 Jan; 11(1):176-81. PubMed ID: 20863902
    [TBL] [Abstract][Full Text] [Related]  

  • 14. DNA sequence analysis of monoamine oxidase B gene coding and promoter regions in Parkinson's disease cases and unrelated controls.
    Costa-Mallen P; Afsharinejad Z; Kelada SN; Costa LG; Franklin GM; Swanson PD; Longstreth WT; Viernes HM; Farin FM; Smith-Weller T; Checkoway H
    Mov Disord; 2004 Jan; 19(1):76-83. PubMed ID: 14743364
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
    Nichols WC; Uniacke SK; Pankratz N; Reed T; Simon DK; Halter C; Rudolph A; Shults CW; Conneally PM; Foroud T;
    Mov Disord; 2004 Jun; 19(6):649-55. PubMed ID: 15197702
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Glucocerebrosidase gene mutations are associated with Parkinson's disease in southern Italy.
    De Marco EV; Annesi G; Tarantino P; Rocca FE; Provenzano G; Civitelli D; Cirò Candiano IC; Annesi F; Carrideo S; Condino F; Nicoletti G; Messina D; Novellino F; Morelli M; Quattrone A
    Mov Disord; 2008 Feb; 23(3):460-3. PubMed ID: 18074383
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of transcription factor polymorphisms PITX3 and EN1 with Parkinson's disease.
    Haubenberger D; Reinthaler E; Mueller JC; Pirker W; Katzenschlager R; Froehlich R; Bruecke T; Daniel G; Auff E; Zimprich A
    Neurobiol Aging; 2011 Feb; 32(2):302-7. PubMed ID: 19345444
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations in NR4A2 associated with familial Parkinson disease.
    Le WD; Xu P; Jankovic J; Jiang H; Appel SH; Smith RG; Vassilatis DK
    Nat Genet; 2003 Jan; 33(1):85-9. PubMed ID: 12496759
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population.
    Cai Y; Ding H; Gu Z; Ma J; Chan P
    Neurosci Lett; 2011 Jul; 498(2):124-6. PubMed ID: 21565251
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Examination of the MASH1 gene in patients with Parkinson's disease.
    Deng H; Yang H; Le W; Deng X; Xu H; Xiong W; Zhu S; Xie W; Song Z; Jankovic J
    Biochem Biophys Res Commun; 2010 Feb; 392(4):548-50. PubMed ID: 20097173
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.